US9629944B2ActiveUtilityA1
Implantable device with a triblock polymer coating
Assignee: ABBOTT CARDIOVASCULAR SYSTEMS INCPriority: Oct 31, 2007Filed: May 20, 2016Granted: Apr 25, 2017
Est. expiryOct 31, 2027(~1.3 yrs left)· nominal 20-yr term from priority
A61L 27/34A61L 2300/606A61L 2420/02A61K 38/13A61L 2300/602A61K 31/436A61K 47/34A61L 2300/416A61L 31/16A61K 38/446A61P 9/00A61K 9/5089A61K 31/33A61K 31/56A61K 45/06A61L 31/10A61K 9/5031A61L 31/148A61K 31/497C08L 67/04C08L 71/02
76
PatentIndex Score
1
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Claims
Abstract
The present invention provides an implantable device having a coating including a slow dissolving polymer or material and the methods of making and using the same.
Claims
exact text as granted — not AI-modifiedThe invention claimed is:
1. An implantable device comprising a coating deposited thereon, the coating comprising a PLGA-PEG-PLGA triblock copolymer;
wherein PLGA in the PLGA-PEG-PLGA triblock copolymer is a block of poly(D,L-lactide-co-glycolide) and PEG in the PLGA-PEG-PLGA triblock copolymer is a block of poly(ethylene glycol);
and
wherein the PLGA-PEG-PLGA triblock copolymer has a weight average molecular weight (M w ) from about 50 KD to about 200 KD and comprises a content of PEG of about 30% or about 40% by weight.
2. The implantable device of claim 1 , wherein the PLGA-PEG-PLGA triblock copolymer has a molecular weight of about 40 KD to about 1000 KD.
3. The implantable device of claim 1 , wherein the content of PEG in the PLGA-PEG-PLGA triblock copolymer is about 30% by weight.
4. The implantable device of claim 1 , wherein the content of PEG in the PLGA-PEG-PLGA triblock copolymer is about 40% by weight.
5. The implantable device of claim 1 , wherein the coating further comprises a bioactive agent.
6. The implantable device of claim 5 , wherein the bioactive agent is selected from the group consisting of paclitaxel, docetaxel, estradiol, 17-beta-estradiol, nitric oxide donors, super oxide dismutases, super oxide dismutases mimics, 4-amino-2,2,6,6-tetramethylpiperidine-1-oxyl (4-amino-TEMPO), biolimus, tacrolimus, dexamethasone, rapamycin, rapamycin derivatives, 40-O-(2-hydroxy)ethyl-rapamycin (everolimus), 40-O-(3-hydroxy)propyl-rapamycin, 40-O-[2-(2-hydroxy)ethoxy]ethyl-rapamycin, 40-O-tetrazole-rapamycin, 40-epi-(N1-tetrazolyl)-rapamycin (ABT-578), γ-hiridun, clobetasol, pimecrolimus, imatinib mesylate, midostaurin, feno fibrate, prodrugs thereof, co-drugs thereof, and combinations thereof.
7. The implantable device of claim 1 , which is a stent.
8. The implantable device of claim 1 , which is a bioabsorbable stent.
9. A method comprising depositing a coating over an implantable device, the coating comprising a PLGA-PEG-PLGA triblock copolymer;
wherein PLGA in the PLGA-PEG-PLGA triblock copolymer is a block of poly(D,L-lactide-co-glycolide) and PEG in the PLGA-PEG-PLGA triblock copolymer is a block of poly(ethylene glycol);
and
wherein the PLGA-PEG-PLGA triblock copolymer has a weight average molecular weight (M w ) from about 50 KD to about 200 KD and comprises a content of PEG of about 30% or about 40% by weight.
10. The method of claim 9 , wherein the content of PEG in the PLGA-PEG-PLGA triblock copolymer is about 30% by weight.
11. The method of claim 9 , wherein the content of PEG in the PLGA-PEG-PLGA triblock copolymer is about 40% by weight.
12. The method of claim 9 , which is a stent.
13. The method of claim 9 , which is a bioabsorbable stent.
14. A method of treating a disorder in a patient, the method comprising implanting in the patient the implantable device according to claim 1 , wherein the disorder is selected from the group consisting of atherosclerosis, thrombosis, restenosis, hemorrhage, vascular dissection, vascular perforation, vascular aneurysm, vulnerable plaque, chronic total occlusion, patent foramen ovale, claudication, anastomotic proliferation for vein and artificial grafts, bile duct obstruction, ureter obstruction, tumor obstruction, and combinations thereof.
15. A method of treating a disorder in a patient, the method comprising implanting in the patient the implantable device according to claim 5 , wherein the disorder is selected from the group consisting of atherosclerosis, thrombosis, restenosis, hemorrhage, vascular dissection, vascular perforation, vascular aneurysm, vulnerable plaque, chronic total occlusion, patent foramen ovale, claudication, anastomotic proliferation for vein and artificial grafts, bile duct obstruction, ureter obstruction, tumor obstruction, and combinations thereof.
16. The implantable device of claim 5 , wherein the bioactive agent is selected from the group consisting of paclitaxel, docetaxel, estradiol, 17-beta-estradiol, nitric oxide donors, super oxide dismutases, 4-amino-2,2,6,6-tetramethylpiperidine-1-oxyl (4-amino-TEMPO), biolimus, tacrolimus, dexamethasone, rapamycin, 40-O-(2-hydroxy)ethyl-rapamycin (everolimus), 40-O-(3-hydroxy)propyl-rapamycin, 40-O-[2-(2-hydroxy)-ethoxy]ethyl-rapamycin, 40-O-tetrazole-rapamycin, 40-epi-(N1-tetrazolyl)-rapamycin (ABT-578), γ-hiridun, clobetasol, pimecrolimus, imatinib mesylate, midostaurin, feno fibrate, and combinations thereof.
17. The implantable device of claim 5 , which is a stent.
18. The implantable device of claim 16 , which is a stent.
19. A method of treating a disorder in a patient, the method comprising implanting in the patient the stent according to claim 17 , wherein the disorder is selected from the group consisting of atherosclerosis, thrombosis, restenosis, hemorrhage, vascular dissection, vascular perforation, vascular aneurysm, vulnerable plaque, chronic total occlusion, patent foramen ovale, claudication, anastomotic proliferation for vein and artificial grafts, bile duct obstruction, ureter obstruction, tumor obstruction, and combinations thereof.
20. A method of treating a disorder in a patient, the method comprising implanting in the patient the stent according to claim 18 , wherein the disorder is selected from the group consisting of atherosclerosis, thrombosis, restenosis, hemorrhage, vascular dissection, vascular perforation, vascular aneurysm, vulnerable plaque, chronic total occlusion, patent foramen ovale, claudication, anastomotic proliferation for vein and artificial grafts, bile duct obstruction, ureter obstruction, tumor obstruction, and combinations thereof.Cited by (0)
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